Clinical heterogeneity of the C9orf72 genetic mutation in frontotemporal dementia.
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| Title: | Clinical heterogeneity of the C9orf72 genetic mutation in frontotemporal dementia. |
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| Authors: | Devenney, E.1,2,3 (AUTHOR) e.devenney@neura.edu.au, Foxe, D.1 (AUTHOR), Dobson-Stone, C.1,4 (AUTHOR), Kwok, J.B.1,4 (AUTHOR), Kiernan, M.C.1,3 (AUTHOR), Hodges, J.R.1,4 (AUTHOR) |
| Source: | Neurocase (Taylor & Francis Ltd). Aug2015, Vol. 21 Issue 4, p535-541. 7p. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 102170984 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=102170984 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1080/13554794.2014.951058 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 7 StartPage: 535 Titles: – TitleFull: Clinical heterogeneity of the C9orf72 genetic mutation in frontotemporal dementia. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Devenney, E. – PersonEntity: Name: NameFull: Foxe, D. – PersonEntity: Name: NameFull: Dobson-Stone, C. – PersonEntity: Name: NameFull: Kwok, J.B. – PersonEntity: Name: NameFull: Kiernan, M.C. – PersonEntity: Name: NameFull: Hodges, J.R. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: Aug2015 Type: published Y: 2015 Identifiers: – Type: issn-print Value: 13554794 Numbering: – Type: volume Value: 21 – Type: issue Value: 4 Titles: – TitleFull: Neurocase (Taylor & Francis Ltd) Type: main |
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